isobavachalcone (Q27103503)

Isobavachalcone (English)

5 October 2016

chemical formula

C₂₀H₂₀O₄

1 reference

Isobavachalcone (English)

5 October 2016

canonical SMILES

CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C

1 reference

Isobavachalcone (English)

5 October 2016

isomeric SMILES

CC(=CCC1=C(C=CC(=C1O)C(=O)/C=C/C2=CC=C(C=C2)O)O)C

1 reference

Two New Benzofuran Derivatives, Corylifonol and Isocorylifonol from the Seeds of Psoralea corylifolia

Isobavachalcone (English)

5 October 2016

7 references

Phytoestrogens from Psoralea corylifolia reveal estrogen receptor-subtype selectivity

Plant antimutagenic agents, 2. Flavonoids.

Antiplatelet flavonoids from seeds of Psoralea corylifolia

Bioactive Metabolites from the Fruits of Psoralea corylifolia

Fingerprint analysis of Psoralea corylifolia L. by HPLC and LC-MS.

Analysis of Psoralea corylifolia L. fruits in different regions

Cullen corylifolia

7 references

Two New Benzofuran Derivatives, Corylifonol and Isocorylifonol from the Seeds of Psoralea corylifolia

Phytoestrogens from Psoralea corylifolia reveal estrogen receptor-subtype selectivity

Plant antimutagenic agents, 2. Flavonoids.

Antiplatelet flavonoids from seeds of Psoralea corylifolia

Bioactive Metabolites from the Fruits of Psoralea corylifolia

Fingerprint analysis of Psoralea corylifolia L. by HPLC and LC-MS.

Analysis of Psoralea corylifolia L. fruits in different regions

Erythrina fusca

1 reference

Flavanoids and pterocarpans from the bark of Erythrina fusca

Sophora prostrata

1 reference

Flavonoids in roots of Sophora prostrata

Moraceae

1 reference

Anti-inflammatory and anticholinesterase activity of six flavonoids isolated from Polygonum and Dorstenia species

Polygonaceae

1 reference

Anti-inflammatory and anticholinesterase activity of six flavonoids isolated from Polygonum and Dorstenia species

Ashitaba

3 references

Chalcones and other compounds from the exudates of Angelica keiskei and their cancer chemopreventive effects

Chalcones from Angelica keiskei

Chalcones, coumarins, and flavanones from the exudate of Angelica keiskei and their chemopreventive effects

Brosimum acutifolium

1 reference

Flavonoids from Brosimum acutifolium

Broussonetia papyrifera

1 reference

Aromatase inhibitors from Broussonetia papyrifera

Dorstenia poinsettifolia

1 reference

Geranylated flavonoids from Dorstenia poinsettifolia

Erythrina burttii

2 references

Three isoflav-3-enes and a 2-arylbenzofuran from the root bark of Erythrina burttii

Two prenylated flavanones from stem bark of Erythrina burttii

Lespedeza cyrtobotrya

1 reference

Melanin synthesis inhibitors from Lespedeza cyrtobotrya

Anthyllis hermanniae

1 reference

Isoflavonoids and chalcones from Anthyllis hermanniae

Glycyrrhiza uralensis

1 reference

Formation of chalcones and isoflavones by callus culture of Glycyrrhiza uralensis with different production patterns.

Hypericum geminiflorum

1 reference

Phenolics from Hypericum geminiflorum

Maclura tinctoria

1 reference

Antifungal chalcones from Maclura tinctoria

Morus cathayana

1 reference

Components of the Root Bark of Morus cathayana. 1. Structures of Five New Isoprenylated Flavonoids, Sanggenols A - E and a Diprenyl-2-arylbenzofuran, Mulberrofuran V

breadfruit

1 reference

Prenylated flavonoids from the heartwood of Artocarpus communis with inhibitory activity on lipopolysaccharide-induced nitric oxide production

Morus alba

2 references

Neuroprotective effect of prenylated arylbenzofuran and flavonoids from morus alba fruits on glutamate-induced oxidative injury in HT22 hippocampal cells

Chemical constituents of Morus alba L. and their inhibitory effect on 3T3-L1 preadipocyte proliferation and differentiation

liquorice

1 reference

Glycybridins A-K, Bioactive Phenolic Compounds from Glycyrrhiza glabra.

Glycyrrhiza inflata

1 reference

Screening for bioactive natural products from a 67-compound library of Glycyrrhiza inflata

Identifiers

InChI

InChI=1S/C20H20O4/c1-13(2)3-9-16-19(23)12-10-17(20(16)24)18(22)11-6-14-4-7-15(21)8-5-14/h3-8,10-12,21,23-24H,9H2,1-2H3/b11-6+

1 reference

Isobavachalcone (English)

5 October 2016

2 references

Isobavachalcone (English)

5 October 2016

ChEBI release 2020-09-01

2 references

isobavachalcone (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=20784-50-3

8 April 2021

1 reference

(2E)-1-[2,4-Dihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-3-(4-hydroxyphenyl)-2-propen-1-one (English)

5 October 2016

2 references

Isobavachalcone (English)

5 October 2016

Reaxys registry number

2004917

1 reference

isobavachalcone (English)

5 October 2016

ChEBI ID

28106

mapping relation type

2 references

isobavachalcone (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C20H20O4/c1-13(2)3-9-16-19(23)12-10-17(20(16)24)18(22)11-6-14-4-7-15(21)8-5-14/h3-8,10-12,21,23-24H,9H2,1-2H3/b11-6+

1 reference

ISOBAVACHALCONE (English)

5 October 2016

2 references

inferred from InChIKey

splash10-014i-0090000000-259f08fca5b685789dd0

1 reference

0 references

DSSTox substance ID

DTXSID601317123

1 reference

0 references

3 references

isobavachalcone (English)

5 October 2016

based on heuristic

inferred from InChIKey

C00036579

2 references

based on heuristic

inferred from InChIKey

UNII

ZWO2SC993A

1 reference